Can inherited cerebellar atrophy ataxia recover?

Updated on healthy 2024-02-28
23 answers
  1. Anonymous users2024-02-06

    1. Cerebellar atrophy and hereditary neurological ataxia are two different things, but cerebellar atrophy will have symptoms of ataxia, and more precisely, cerebellar atrophy is not a disease, but neuroimaging manifestations. Hereditary ataxia is a disease caused by inherited genes, and cerebellar atrophy are two different things, and the two cannot be equated.

    2. Cerebellar atrophy and hereditary ataxia, the two are not the same, so there will be differences in the above, although both have symptoms of ataxia, but at the time, it is necessary to find out the cause of the disease, so it is different in all aspects such as medication and medication, and it is recommended that patients should go to a regular hospital to receive the corresponding **.

    3. At the same time as the patient is taking medication, he must carry out the first for cognitive function and mental disorders, you should self-adjust in the psychological aspect, if not, you should find a psychologist to help, you should build a confidence in the disease, as well as self-training, etc., to overcome some negative psychological states.

    Precautions: Hereditary ataxia can actually be prevented, that is, to avoid consanguineous marriage, if the patient carries this gene, can take elective abortion. Generally speaking, patients with ataxia can get it as long as they pass, train and systematize, and should have confidence in it.

  2. Anonymous users2024-02-05

    This is mainly to control the disease, and the hereditary is not the best, and the main thing is to improve.

  3. Anonymous users2024-02-04

    Hereditary cerebellar atrophy ataxia can not be **, but the condition can be improved by drinking Chinese medicine.

  4. Anonymous users2024-02-03

    Ataxia refers to a disorder of coordination of movement with normal muscle strength. Disturbance of the amplitude and coordination of voluntary movements of the limbs, and inability to maintain body posture and balance. However, it does not include coordination impairment in mild limb paralysis, voluntary movement deviation due to ophthalmoplegia, difficulty in voluntary movement due to visual impairment, and apraxia due to cerebral lesions.

    Depending on the location of the lesion, ataxia can be divided into four types: deep sensory impairment ataxia; cerebellar ataxia; vestibular labyrinthine ataxia; Cerebral ataxia. The commonly known as "ataxia" refers to cerebellar ataxia.

  5. Anonymous users2024-02-02

    This is mainly about controlling the disease.

  6. Anonymous users2024-02-01

    You can try Chinese medicine**.

  7. Anonymous users2024-01-31

    There is currently no particularly good way to cure this type of disease. At present, the main thing is to control the further aggravation of the disease through drugs, and to improve the corresponding clinical symptoms on the basis of corresponding functional training. Generally speaking, it is hereditary, you can take some drugs to nourish the nerves, such as vitamin B, try to pay attention to rest, live a regular life, and avoid overwork.

  8. Anonymous users2024-01-30

    There is no cure for ataxia, but as long as the patient cooperates with the doctor and exercises more, the complications will be relatively mild.

    Ataxia can be caused by a variety of causes, but the most common ataxia is a hereditary, cerebellar ataxia disorder that is the result of inherited genetic variation. In addition, ataxia is caused by damage to the brain, cerebellum or other parts, deep sensation or vestibular damage. As the injury is relieved and neurological function slowly recovers, ataxia may return to a certain extent.

    Patients can seek the help of a professional teacher to relieve the tension, anxiety, pessimism, depression and other emotions of the disease, and enhance their confidence in overcoming the disease.

  9. Anonymous users2024-01-29

    This can only be controlled.

  10. Anonymous users2024-01-28

    The patient with cerebellar atrophy ataxia is 38 years old, with the disease for about 4 years, and the main symptoms are: insomnia, dreaminess, easy to wake up, eating and making ulnal holes, drinking water and choking, dizziness and headache, difficulty swallowing, slow speech, slurred speech, unsteady walking, unsteady standing, shaky walking, weakness of the lower limbs, stiffness of limbs, difficulty in urinating and urinating and other symptoms.

    The patient did not have a way at first, in a chance to learn that the effect of the brain walking soup is good, the appointment of the doctor of the dialectical prescription of a course of drugs, headache and dizziness, insomnia, dreaminess and other conditions have improved after the medication, the patient feels that the effect is good, the patient continues to adjust the second and third courses of drugs, after the medication walking unsteadily, unsteady standing, difficulty swallowing, drinking water and choking cough have improved, the patient continues to adjust the symptoms after five courses of dry drugs, and now everything is normal in the return visit.

  11. Anonymous users2024-01-27

    Cerebellar atrophy, also known as spinocerebellar atrophy, is a family dominant neurological disease, and only one of the parents will have a 50% chance of inheriting the disease. Considerations for patients with cerebellar atrophy:

    1) Daily life: 1. Life must be regular, go to bed early and get up early, and do not stay up late. 2. Don't fix the posture of holding jujube for too long, and you should often change your posture and mode of activity.

    3. If you are too tired from activities throughout the day, try to rest in bed for a while at noon. However, if you don't sleep well at night, don't take too long a nap in the middle of the day. 4. Arrange some routine things to do every day, so that you have to work hard to complete the task, a little difficult is better, such as entertainment, work, etc., can improve morale, create joy in life or a sense of achievement.

    5. Go to bed early and get up early in spring and summer, and go to bed late and get up late in autumn and winter, so as to adapt to the four seasons of climate change in nature.

    2) Healthy diet: 1. Don't be too particular about your diet, preferably in natural food forms. Don't over-process and the fewer food additives the better.

    2. Eat a variety of vegetables and fruits in rotation to absorb different nutrients. 1 egg, 2 large cups of milk per day. Eat more fish and seafood, moderate meat and soy products.

    Do not eat fried, puff pastry, spicy, pickled, canned soups, cream, tomato pulp, sausages, bacon, hot dogs, cakes, potato chips. Coffee, cigarettes, alcohol, and tea should also be used sparingly. The best ones are pure water and fresh fruit juices.

    3. The diet should be low in salt, sugar and fat. 4. Nutrition should be balanced, don't overeat.

  12. Anonymous users2024-01-26

    This is not good ** if it can be fully recovered. In the patient's condition, physical exercises and other physical exercises can be considered to improve the patient's symptoms or delay the progression of the disease.

    Cerebellar atrophy is an imaging finding, not specifically a disease.

    Hereditary diseases, neurodegenerative diseases, bad habits, poisoning, degenerative diseases, hypoxia, intracranial infection, Chibiosis, etc. may cause cerebellar atrophy. Patients can go to the hospital**physiotherapy department or neurology department for follow-up** according to the doctor's instructions**.

    Inherited cerebellar ataxia is generally not curable. There is currently no effective method for hereditary cerebellar ataxia, functional training or oral medication can be used to delay disease progression, but it cannot. Hereditary cerebellar ataxia is mainly about prevention, it is a hereditary disease, and those with a family history should try not to have children after marriage, and do not marry close relatives.

    In hereditary cerebellar ataxia, some patients may have difficulty walking, so it is necessary to prevent falls and be accompanied by someone as much as possible. Usually the diet should be balanced and reasonable, and there should be enough protein and vitamin intake. Dysfunction occurs because of the deterioration of cerebellar function in the brain.

    Ataxia can be called the more familiar cerebellar atrophy. The cerebellum is an important coordination center in the body, and its left and right hemispheres have their own functions. Ataxia can also be caused by the dysfunction of the cerebellum to transmit signals to various parts, and the human limbs cannot feedback the sense of movement to the cerebellum, and only with the patency of the afferent and efferent nerves of the cerebellum and the participation of the corresponding cells can the human body complete accurate movements and maintain correct posture.

    Ataxia is a chronic disease in which the feet are involuntarily separated and swaying when walking, and it is difficult to sit firmly when the disease is more severe, and the direction of the body falling on different vermisites will be different. In addition to physical impairment, there may also be poetic or explosive speech disorders. The eye can also oscillate uncontrollably back and forth due to gross ataxia nystagmus caused by ataxia.

    In the case of acute cerebellar lesions, there is also a rapid decrease in muscle tone.

    Ataxia is not terrible, it is a disease that can be abridged, but everyone's physical condition is different, and the time required is also different, the sooner it is detected, the easier it will be, and the sooner you can make your body return to normal as soon as possible. No matter what the disease is, you can't have a fluke mentality, the disease will not get better on its own, and it can only be cured through **. Don't be too depressed when you're in **, and keep a regular life.

  13. Anonymous users2024-01-25

    Hereditary cerebellar spinal cord ataxia is a congenital genetic disease, **relatively speaking, there is no good way, only symptomatic**, patients are prone to dizziness, unsteady walking and other symptoms, will also be accompanied by slurred speech, there will be poetry-like language. At present, in this case, try to take drugs to improve brain metabolism to alleviate the patient's symptoms, but not completely, only to improve the symptoms.

  14. Anonymous users2024-01-24

    Um, still wearing sex um, still wearing sex cerebellar atrophy, all uh attack disorder, can it be recovered? Can hereditary cerebellar atrophy, can it be cured? But it also takes time um, and the cerebellar atrophy of the penetrating sex, all uh attack disorder, can it be recovered?

    Can hereditary cerebellar atrophy, can it be cured? But it also takes time, because it must be very difficult in the process now, but it can be cured.

  15. Anonymous users2024-01-23

    Hereditary cerebellar atrophy, ataxia, can it be recovered? I think it should be able to recover, but I still need to consult an expert about this.

  16. Anonymous users2024-01-22

    Hereditary cerebellar atrophy, ataxia can be recovered, right? I think it's very difficult to recover from this disease because he also has some nerve fibers on his hands.

  17. Anonymous users2024-01-21

    For this disease, its recovery is relatively difficult, and this recovery index is relatively low, so it is better to accompany it as much as possible.

  18. Anonymous users2024-01-20

    Whether it can be recovered depends on the individual's will, or that sentence, don't be arrogant, don't indulge in the case that the patient's family should have protective measures, try to let the patient exercise and exercise actively, and maintain an optimistic attitude to restore the operation of the brain through self-exercise, and let the patient actively use the brain, so that the brain can recover to a better state on its own, isn't it?

  19. Anonymous users2024-01-19

    In such a situation, if it is hereditary, then it should be impossible to recover, and can only be controlled by drugs, and the hereditary one cannot be **.

  20. Anonymous users2024-01-18

    The main symptoms of cerebral atrophy are: memory loss, slurred speech, impaired comprehension and emotion, dementia and ataxia (unstable balance, left and left swaying walking, tilting back and forth, dizziness, intention tremor), and weakness of the feet.

  21. Anonymous users2024-01-17

    In the case of cerebellar atrophy ataxia, which is usually caused by hereditary diseases, then there is no particularly good way, and some drugs that nourish the nerves, such as gamma oryzanol and vitamin B1, can be improved. Moreover, we should pay attention to rest, avoid strenuous exercise, pay attention to the rules of life, adjust our mentality, and actively supplement various nutrients.

  22. Anonymous users2024-01-16

    Cerebellar atrophy may be triggered by neurodegenerative diseases, bad lifestyle habits, poisoning, degenerative diseases, hypoxia, and intracranial infectious diseases.

  23. Anonymous users2024-01-15

    Hereditary cerebellar atrophy ataxia, there is currently no good way to ** disease, mainly to take drugs to control the aggravation of the disease, and then cooperate with the corresponding functional training, plus acupuncture, massage, etc.

    You can also take some drugs such as neuronutrition, live a regular life, avoid overwork, and pay more attention to rest. Patients should not put pressure on themselves, let alone be nervous, otherwise it will cause fatigue of brain cells, atrophy and forgetfulness. You can't drink too much alcohol, smoke excessively, and don't be deficient in vitamins.

    Maintaining a good mood, participating in regular physical exercise, developing good living habits, and eating more nut foods will play a great role in the control of the disease.

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